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rs34805604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs34805604(A;G)
Make rs34805604(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position40299125
GeneLRRK2
is asnp
is mentioned by
dbSNPrs34805604
ebirs34805604
HLIrs34805604
Exacrs34805604
Varsomers34805604
Maprs34805604
PheGenIrs34805604
hapmaprs34805604
1000 genomesrs34805604
hgdprs34805604
ensemblrs34805604
gopubmedrs34805604
geneviewrs34805604
scholarrs34805604
googlers34805604
pharmgkbrs34805604
gwascentralrs34805604
openSNPrs34805604
23andMers34805604
23andMe allrs34805604
SNP Nexus

SNPshotrs34805604
SNPdbers34805604
MSV3drs34805604
GWAS Ctlgrs34805604
Max Magnitude0
OMIM609007
Desc
Variant0005
Relatedalso


ClinVar
Risk rs34805604(G;G)
Alt rs34805604(G;G)
Reference rs34805604(A;A)
Significance Pathogenic
Disease Parkinson disease 8
Variation info
Gene LRRK2
CLNDBN Parkinson disease 8, autosomal dominant
Reversed 0
HGVS NC_000012.11:g.40692927A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002016.2,



[PMID 15541309] Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.